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Biomimetic Total Synthesis of Hyperjapones A–E and Hyperjaponols A and C

https://doi.org/10.1002/anie.201606091
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ange.201502302openalex-snapshot
Where is the Oxygen? Structural Analysis of α‐Humulene Oxidation Products by the Crystalline Sponge Method
inferredcites →https://doi.org/10.1002/anie.201502302openalex-snapshot
Where is the Oxygen? Structural Analysis of α‐Humulene Oxidation Products by the Crystalline Sponge Method
inferredcites →https://doi.org/10.1002/chem.201200619openalex-snapshot
ortho‐Quinone Methides in Natural Product Synthesis
inferredcites →https://doi.org/10.1016/0040-4020(96)00367-5openalex-snapshot
The cleavage of caryophyllene oxide catalysed by tetracyanoethylene
inferredcites →https://doi.org/10.1016/j.tet.2009.06.017openalex-snapshot
Novel cyclopeptide and unique flavone from Desmos rostrata. Total synthesis of desmorostratone
inferredcites →https://doi.org/10.1016/j.tet.2016.01.004openalex-snapshot
Chromatography with silver nitrate: part 2
inferredcites →https://doi.org/10.1016/s0031-9422(00)00266-1openalex-snapshot
The role of germacrene D as a precursor in sesquiterpene biosynthesis: investigations of acid catalyzed, photochemically and thermally induced rearrangements
inferredcites →https://doi.org/10.1016/s0040-4020(00)00927-3openalex-snapshot
Chromatography with silver nitrate
inferredcites →https://doi.org/10.1016/s0040-4020(02)00496-9openalex-snapshot
o-Quinone methides: intermediates underdeveloped and underutilized in organic synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)71413-4openalex-snapshot
Rearrangement of humulene-8,9-epoxide
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00968openalex-snapshot
Nortriketones: Antimicrobial Trimethylated Acylphloroglucinols from Manuka (Leptospermum scoparium)
inferredcites →https://doi.org/10.1021/acs.orglett.5b01973openalex-snapshot
Total Synthesis and Structure Revision of (−)-Siphonodictyal B and Its Biomimetic Conversion into (+)-Liphagal
inferredcites →https://doi.org/10.1021/acs.orglett.6b00650openalex-snapshot
Hyperjapones A–E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum
inferredcites →https://doi.org/10.1021/acs.orglett.6b00906openalex-snapshot
Filicinic Acid Based Meroterpenoids with Anti-Epstein–Barr Virus Activities from Hypericum japonicum
inferredcites →https://doi.org/10.1021/ar500330xopenalex-snapshot
The Domestication of ortho -Quinone Methides
inferredcites →https://doi.org/10.1021/jacs.5b11438openalex-snapshot
Total Synthesis of (+)-Cytosporolide A via a Biomimetic Hetero-Diels–Alder Reaction
inferredcites →https://doi.org/10.1021/jo00892a023openalex-snapshot
Acid-catalyzed rearrangements of humulene
inferredcites →https://doi.org/10.1021/ol100138kopenalex-snapshot
A Short Biomimetic Synthesis of the Meroterpenoids Guajadial and Psidial A
inferredcites →https://doi.org/10.1021/ol101380aopenalex-snapshot
Biomimetic Synthesis of Polycyclic Polyprenylated Acylphloroglucinol Natural Products Isolated from Hypericum papuanum
inferredcites →https://doi.org/10.1021/ol202181gopenalex-snapshot
Structural Reassignment of Cytosporolides A–C via Biomimetic Synthetic Studies and Reinterpretation of NMR Data
inferredcites →https://doi.org/10.1021/ol202641yopenalex-snapshot
Efficient Generation of ortho-Quinone Methide: Application to the Biomimetic Syntheses of (±)-Schefflone and Tocopherol Trimers
inferredcites →https://doi.org/10.1021/ol302849vopenalex-snapshot
Isolation and Biomimetic Synthesis of (±)-Guajadial B, a Novel Meroterpenoid from Psidium guajava
inferredcites →https://doi.org/10.1021/ol991068qopenalex-snapshot
A Biomimetic Synthesis of Lucidene
inferredcites →https://doi.org/10.1039/b508972gopenalex-snapshot
A new and efficient method for o-quinone methide intermediate generation: application to the biomimetic synthesis of the benzopyran derived natural products (±)-lucidene and (±)-alboatrin
inferredcites →https://doi.org/10.1039/b917107jopenalex-snapshot
The carbocation continuum in terpene biosynthesis—where are the secondary cations?
inferredcites →https://doi.org/10.1039/c1np00006copenalex-snapshot
Biosynthesis via carbocations: Theoretical studies on terpene formation
inferredcites →https://doi.org/10.1039/p19740001598openalex-snapshot
Acid-catalysed cyclisation of humulene
inferredcites →https://doi.org/10.1039/p19870000317openalex-snapshot
Synthesis of the Mammea coumarins. Part 1. The coumarins of the mammea A, B, and C series
inferredcites →https://doi.org/10.1039/p19870000353openalex-snapshot
Synthesis of the Mammea coumarins. Part 4. Stereochemical and regiochemical studies, and synthesis of (–)-mammea B/BB
inferredcites →https://doi.org/10.1246/cl.1973.133openalex-snapshot
ACID CATALYZED ISOMERIZATION OF HUMULENE (PART 1)
inferredcites →https://doi.org/10.1246/cl.1973.727openalex-snapshot
ACID CATALYZED ISOMERIZATION OF HUMULENE (PART 2) STEREOCHEMISTRY AND THE REACTION PATHWAYS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113308zenodo-depositor-declared
Hyjapones A−D, trimethylated acyphloroglucinol meroterpenoids from Hypericum japonicum thunb. With anti-inflammatory activity
inferred← citeshttps://doi.org/10.2139/ssrn.4666804openalex-extracted
Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/ange.201804351openalex-snapshot
Total Synthesis Establishes the Biosynthetic Pathway to the Naphterpin and Marinone Natural Products
inferred← citeshttps://doi.org/10.1002/ange.201814421openalex-snapshot
Isolation and Synthesis of Novel Meroterpenoids from Rhodomyrtus tomentosa: Investigation of a Reactive Enetrione Intermediate
inferred← citeshttps://doi.org/10.1002/ange.202312568openalex-snapshot
Biomimetic Synthesis of an Antiviral Cinnamoylphloroglucinol Collection from Cleistocalyx operculatus: A Synthetic Strategy Based on Biogenetic Building Blocks
inferred← citeshttps://doi.org/10.1002/ange.202400515openalex-snapshot
Enantioselective Hydrofunctionalization of Cyclobutenones: Total Synthesis of gem‐Dimethylcyclobutane Natural Products
inferred← citeshttps://doi.org/10.1002/anie.201804351openalex-snapshot
Total Synthesis Establishes the Biosynthetic Pathway to the Naphterpin and Marinone Natural Products
inferred← citeshttps://doi.org/10.1002/anie.201814421openalex-snapshot
Isolation and Synthesis of Novel Meroterpenoids from Rhodomyrtus tomentosa: Investigation of a Reactive Enetrione Intermediate
inferred← citeshttps://doi.org/10.1002/anie.202312568openalex-snapshot
Biomimetic Synthesis of an Antiviral Cinnamoylphloroglucinol Collection from Cleistocalyx operculatus: A Synthetic Strategy Based on Biogenetic Building Blocks
inferred← citeshttps://doi.org/10.1002/anie.202400515openalex-snapshot
Enantioselective Hydrofunctionalization of Cyclobutenones: Total Synthesis of gem‐Dimethylcyclobutane Natural Products
inferred← citeshttps://doi.org/10.1002/chem.202001111openalex-snapshot
Discovery and Biomimetic Synthesis of a Phloroglucinol‐Terpene Adduct Collection from Baeckea frutescens and Its Biogenetic Origin Insight
inferred← citeshttps://doi.org/10.1002/chem.202001405openalex-snapshot
Discoveries and Challenges en Route to Swinhoeisterol A
inferred← citeshttps://doi.org/10.1002/chem.202203425openalex-snapshot
Pro‐aromaticity Enabled Dealkenylative Functionalizations via Photo‐Excitation and Oxidation
inferred← citeshttps://doi.org/10.1002/chem.202500819openalex-snapshot
Xanthochrysanthones A−C, Novel Lobster‐Shape Cinnamoyltriketone Dimers with Antiviral Activities from Xanthostemon chrysanthus
inferred← citeshttps://doi.org/10.1007/s11101-019-09646-8openalex-snapshot
Chemical synthesis of terpenoids with participation of cyclizations plus rearrangements of carbocations: a current overview
inferred← citeshttps://doi.org/10.1016/j.tchem.2022.100013openalex-snapshot
Enzymatic intermolecular Diels-Alder reactions in synthesis: From nature to design
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2017.05.007openalex-snapshot
Biomimetic synthesis of myrtucommulone K, N and O
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.058openalex-snapshot
Hyperjapones F–I, terpenoid polymethylated acylphloroglucinols from Hypericum japonicum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155080openalex-snapshot
Biomimetic syntheses of myrtucommulones K-L and N, and callistiviminenes F-H
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00019openalex-snapshot
Biomimetic Dearomatization Strategies in the Total Synthesis of Meroterpenoid Natural Products
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.8b00283openalex-snapshot
Nature-Inspired Bioorthogonal Reaction: Development of β-Caryophyllene as a Chemical Reporter in Tetrazine Ligation
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00653openalex-snapshot
Divergent Strategy in Natural Product Total Synthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00131openalex-snapshot
Discovery of Dual-Target Anti-Alzheimer’s Filicinic Acid-Based Meroterpenoids from Hypericum japonicum Thunb.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01077openalex-snapshot
The First Racemic Total Syntheses of the Antiplasmodials Watsonianones A and B and Corymbone B
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02643openalex-snapshot
Frutescone A–G, Tasmanone-Based Meroterpenoids from the aerial parts of Baeckea frutescens
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01050openalex-snapshot
Phloroglucinol Derivatives with Unusual Skeletons from Cleistocalyx operculatus and Their in Vitro Antiviral Activity
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02968openalex-snapshot
Total Synthesis of Rhodonoids A, B, E, and F, Enabled by Singlet Oxygen Ene Reactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03156openalex-snapshot
Biomimetic Synthesis Enables the Structure Revision of Littordials E and F and Drychampone B
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00560openalex-snapshot
Enantiospecific Total Synthesis of (−)-Japonicol C
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01616openalex-snapshot
Rhodomentosones A and B: Two Pairs of Enantiomeric Phloroglucinol Trimers from Rhodomyrtus tomentosa and Their Asymmetric Biomimetic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01175openalex-snapshot
Total Synthesis of Eucalyptusdimers A–C
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02159openalex-snapshot
Biomimetic-Inspired Syntheses of Myrtucommuacetalone and Myrtucommulone J
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03815openalex-snapshot
Biomimetic Total Syntheses of Callistrilones A, B, and D
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03158openalex-snapshot
Catalytic Asymmetric Hydrophosphination of ortho-Quinone Methides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04003openalex-snapshot
A General Biomimetic Hetero-Diels–Alder Approach to the Core Skeletons of Xenovulene A and the Sterhirsutins A and B
inferred← citeshttps://doi.org/10.1021/acscentsci.6b00293openalex-snapshot
Unravelling Photochemical Relationships Among Natural Products from Aplysia dactylomela
inferred← citeshttps://doi.org/10.1021/jacs.2c09978openalex-snapshot
Total Synthesis of Atrachinenins A and B
inferred← citeshttps://doi.org/10.1021/jacs.9b10474openalex-snapshot
Chemoenzymatic o -Quinone Methide Formation
inferred← citeshttps://doi.org/10.1021/jacsau.5c00201openalex-snapshot
Total Synthesis of (−)-Elodeoidins A and B
inferred← citeshttps://doi.org/10.1038/s41598-017-01028-4openalex-snapshot
Psiguajadials A–K: Unusual Psidium Meroterpenoids as Phosphodiesterase-4 Inhibitors from the Leaves of Psidium guajava
inferred← citeshttps://doi.org/10.1039/c6cs00935bopenalex-snapshot
Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis
inferred← citeshttps://doi.org/10.1039/c7ob00868fopenalex-snapshot
Biosynthetically-inspired oxidations of capillobenzopyranol
inferred← citeshttps://doi.org/10.1039/c7qo00678kopenalex-snapshot
Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence
inferred← citeshttps://doi.org/10.1039/c7sc04672copenalex-snapshot
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E
inferred← citeshttps://doi.org/10.1039/c8cs00274fopenalex-snapshot
Recent advances in the application of Diels–Alder reactions involving o -quinodimethanes, aza- o -quinone methides and o -quinone methides in natural product total synthesis
inferred← citeshttps://doi.org/10.1039/c8ob01092gopenalex-snapshot
Biomimetic total syntheses of chromane meroterpenoids, guadials B and C, guapsidial A and psiguajadial D
inferred← citeshttps://doi.org/10.1039/c8ob02433bopenalex-snapshot
Atropisomeric meroterpenoids with rare triketone-phloroglucinol-terpene hybrids from Baeckea frutescens
inferred← citeshttps://doi.org/10.1039/c8ob02687dopenalex-snapshot
Meroterpene-like compounds derived from β-caryophyllene as potent α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1039/c8qo00130hopenalex-snapshot
Asymmetric total syntheses of callistrilones B, G and J
inferred← citeshttps://doi.org/10.1039/c9np00037bopenalex-snapshot
Naturally occurring [4 + 2] type terpenoid dimers: sources, bioactivities and total syntheses
inferred← citeshttps://doi.org/10.1039/c9ob02490eopenalex-snapshot
Biomimetic total syntheses of baefrutones A–D, baeckenon B, and frutescones A, D–F
inferred← citeshttps://doi.org/10.1039/d1np00077bopenalex-snapshot
Recent advances in the synthesis of natural products containing the phloroglucinol motif
inferred← citeshttps://doi.org/10.1039/d1ob00693bopenalex-snapshot
Psidguajones A and B, a pair of complex meroterpenoid epimers from the leaves of Psidium guajava
inferred← citeshttps://doi.org/10.1039/d2cc01398copenalex-snapshot
Bioinspired enantioselective total syntheses of antibacterial callistrilones enabled by double S N 2′ cascade
inferred← citeshttps://doi.org/10.1039/d2ob00074aopenalex-snapshot
Biomimetic synthesis of the non-canonical PPAP natural products yezo'otogirin C and hypermogin D, and studies towards the synthesis of norascyronone A
inferred← citeshttps://doi.org/10.1039/d2qo00792dopenalex-snapshot
Bio-inspired construction of a tetracyclic ring system with an avarane skeleton: total synthesis of dactyloquinone A
inferred← citeshttps://doi.org/10.1055/a-1917-7910openalex-snapshot
Antimicrobial Acylphloroglucinol Meroterpenoids and Acylphloroglucinols from Dryopteris crassirhizoma
inferred← citeshttps://doi.org/10.1071/ch18141openalex-snapshot
Biomimetic Synthesis of Hyperjapones F-I
inferred← citeshttps://doi.org/10.17344/acsi.2021.6921openalex-snapshot
Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids
inferred← citeshttps://doi.org/10.26434/chemrxiv.7828769.v1openalex-snapshot
Biocatalyst-Initiated Ortho-Quinone Methide Formation and Derivatization
inferred← citeshttps://doi.org/10.3390/ijms252111435openalex-snapshot
1,3-Dipolar Cycloaddition of Nitrile Oxides and Nitrilimines to (−)-β-Caryophyllene: Stereoselective Synthesis of Polycyclic Derivatives and Their Biological Testing
inferred← citeshttps://doi.org/10.3390/molecules25020260openalex-snapshot
Meroterpene-Like α-Glucosidase Inhibitors Based on Biomimetic Reactions Starting from β-Caryophyllene
inferred← citeshttps://doi.org/10.3390/plants13182668openalex-snapshot
Insights into Chemical Diversity and Potential Health-Promoting Effects of Ferns
inferred← citeshttps://doi.org/10.3762/bjoc.22.21openalex-snapshot
Ring contraction and ring expansion reactions in terpenoid biosynthesis and their application to total synthesis
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